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- 欧洲议会和欧洲委员会体外诊断医疗器械指令 Directive of the European Parliament and of the Council on in Vitro Diagnostic Medical Devices
- 实验室试验和体外诊断试验系统专业人员用体外诊断试验医疗器械厂商提供信息调整要求概要 Clinical laboratory testing and in vitro diagnostic test systems - In vitro diagnostic medical devices for professional use - Summary of regulatory requirements for information supplied by the manufacturer
- 离体诊断医疗器械指令 in vitro diagnostic medical device directive
- 体外诊断试剂 in vitro diagnostic reagent
- 体外诊断用血库离心机 Blood bank centrifuge for in vitro diagnostic use
- 基于核酸的体外诊断 Nueleie acid-based IVDs
- 体外诊断用的强化培养基 Potentiating media for in vitro diagnostic use
- 体外诊断试剂管理亟待加强 Management of Diagnosis Regents should Strengthened
- 体外受孕 vitro fertilization
- 体外诊断 in vitro diagnosis(IVD)
- 体外标记 in vitro labelling; labelled in vitro
- 体外测定 in vitro assay
- 体外超滤 extra-corporeal ultrafiltration
- 体外除颤 external defibrillation
- 体外磁铁 external magnet
- 体外复温 external rewarming
- 体外灌注 ECP; extracorporeal perfusion
- 体外活体 supravital
- 体外计数 in vitro counting; surface counting
- 体外接管 extracorporeal tubing
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